Intrinsic Factor antibody (AA 189-218)

Catalog No. ABIN7871523

The Rabbit Polyclonal anti-Intrinsic Factor antibody is suitable to detect Intrinsic Factor in samples from Human. It has been validated for WB, IF, FACS and IHC (p).

Quick Overview for Intrinsic Factor antibody (AA 189-218) (ABIN7871523)

Target: Intrinsic Factor (GIF) (Gastric Intrinsic Factor (Vitamin B Synthesis) (GIF))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Intrinsic Factor antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-Intrinsic Factor Antibody

Binding Specificity: AA 189-218

Purpose: Gastric Intrinsic Factor Antibody / GIF / CBLIF

Purification: Antigen affinity purified

Immunogen: A portion of amino acids 189-218 from the human protein was used as the immunogen for the Gastric Intrinsic Factor antibody.

Isotype: Ig Fraction

Application Details

Application Notes: The stated application concentrations are suggested starting points. Titration of the Gastric Intrinsic Factor antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Aliquot the Gastric Intrinsic Factor antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Target Details for Intrinsic Factor

Target: Intrinsic Factor (GIF) (Gastric Intrinsic Factor (Vitamin B Synthesis) (GIF))

Alternative Name: Gastric Intrinsic Factor

Background: This gene is a member of the cobalamin transport protein family. It encodes a glycoprotein secreted by parietal cells of the gastric mucosa and is required for adequate absorption of vitamin B12. Vitamin B12 is necessary for erythrocyte maturation and mutations in this gene may lead to congenital pernicious anemia.

UniProt: P27352